Matrix Attachment Region Binding Proteins
"Matrix Attachment Region Binding Proteins" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Proteins that bind to the MATRIX ATTACHMENT REGIONS of DNA.
| Descriptor ID |
D036961
|
| MeSH Number(s) |
D12.776.260.532
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Matrix Attachment Region Binding Proteins".
Below are MeSH descriptors whose meaning is more specific than "Matrix Attachment Region Binding Proteins".
This graph shows the total number of publications written about "Matrix Attachment Region Binding Proteins" by people in this website by year, and whether "Matrix Attachment Region Binding Proteins" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 2000 | 2 | 0 | 2 |
| 2005 | 1 | 0 | 1 |
| 2007 | 1 | 0 | 1 |
| 2009 | 4 | 0 | 4 |
| 2010 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 1 | 2 |
| 2019 | 1 | 0 | 1 |
| 2020 | 2 | 0 | 2 |
| 2021 | 2 | 0 | 2 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Matrix Attachment Region Binding Proteins" by people in Profiles.
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Pathogenic SATB2 missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypes. J Med Genet. 2024 Oct 23; 61(11):1062-1067.
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PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework. Nat Genet. 2023 09; 55(9):1598-1607.
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SATB2 Expression in Undifferentiated Pleomorphic Sarcomas of Bone. Am J Clin Pathol. 2022 08 04; 158(2):235-241.
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Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction. Am J Hum Genet. 2021 02 04; 108(2):346-356.
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Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2. Clin Genet. 2021 04; 99(4):547-557.
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Immunohistochemical Expression of CDX2 and SATB2 in Primary Breast Carcinomas. Appl Immunohistochem Mol Morphol. 2020 07; 28(6):e53.
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Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated Syndrome. Pediatr Neurol. 2020 11; 112:94-100.
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Mutation update for the SATB2 gene. Hum Mutat. 2019 08; 40(8):1013-1029.
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Molecular Fingerprinting of On-Off Direction-Selective Retinal Ganglion Cells Across Species and Relevance to Primate Visual Circuits. J Neurosci. 2019 01 02; 39(1):78-95.
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Interobserver Reproducibility Among Gynecologic Pathologists in Diagnosing Heterologous Osteosarcomatous Component in Gynecologic Tract Carcinosarcomas. Int J Gynecol Pathol. 2017 Jul; 36(4):386-392.